Our long term goal is to identify mechanisms of cellular long chain free fatty acid (LCFFA) uptake and their possible roles in disease. Our earlier work helped prove that the major LCFFA uptake process under physiologic conditions is facilitated transport showed altered tissue specific regulation of this process in adipocytes in a rat model of obesity and type 2 diabetes and hepatocytes during exposure to ethanol and isolated the first plasma membrane LCFFA transporter) which, surprisingly, proved identical to mitochondrial aspartate aminotransferase (mAspAT). During the 1998-2002 funding period, we showed: [1] that tissue-specific up-regulation of adipocyte LCFFA uptake was characteristic of both genetic and dietary obesity in several additional rodent models and adipocytes from obese human subjects; [2] that the extent of up-regulation was closely correlated with the rate of weight gain in a rat model of dietary obesity; and [3] that up-regulation or down-regulation of facilitated LCFFA uptake in adipocytes preceded weight gain or weight loss, respectively, in several experimental settings, suggesting that regulation of adipocyte LCFFA uptake is an important control point for body adiposity. In one such study, administration of leptin to hyperinsulinemic ob/ob mice led sequentially to a rapid fall in plasma insulin levels, a progressive decrease in the rate of facilitated LCFFA uptake by adipocytes, decreased food intake, weight loss, and finally, a decrease in the size of adipocytes and of passive LCFFA uptake. These data suggest that insulin is an up-regulator and leptin a downregulator of adipocyte LCFFA uptake, but leave open the question of whether the leptin effect is direct or is mediated by its influence on insulin secretion and function. The current application seeks to build on these observations.
SPECIFIC AIM 1 seeks to confirm the relationship between the extent of up-regulation of uptake and the rate of weight gain, and to verify that the observed changes in adipocyte LCFFA uptake result in changes in nutrient partitioning in the Osborne-Mendel rat, which is sensitive to diet-induced obesity.
SPECIFIC AIM 2 is to clarify the roles of insulin and leptin in respectively up- and down-regulating adipocyte LCFFA uptake. In studies proposed for SPECIFIC AIM 3 we will use adipocyte culture systems to examine the effects of hormones and other potential regulators of adipocyte LCFFA uptake, and explore the effects of RNA silencing of putative LCFFA transporters on LCFFA uptake and triglycerides accumulation. Finally, SPECIFIC AIM 4 will characterize depotspecific differences in LCFFA uptake in freshly isolated human adipocytes removed at surgery, and will also determine the effects of massive weight loss resulting from bariatric surgical interventions on these transport processes. Since tissue-specific up-regulation of LCFFA uptake characterizes obesity, understanding the regulatory mechanisms may have therapeutic implications.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Research Project (R01)
Project #
5R01DK052401-09
Application #
7250089
Study Section
Nutrition Study Section (NTN)
Program Officer
Yanovski, Susan Z
Project Start
1998-01-01
Project End
2009-06-30
Budget Start
2007-07-01
Budget End
2008-06-30
Support Year
9
Fiscal Year
2007
Total Cost
$335,846
Indirect Cost
Name
Columbia University (N.Y.)
Department
Internal Medicine/Medicine
Type
Schools of Medicine
DUNS #
621889815
City
New York
State
NY
Country
United States
Zip Code
10032
Berk, Paul D; Verna, Elizabeth C (2016) Nonalcoholic Fatty Liver Disease: Lipids and Insulin Resistance. Clin Liver Dis 20:245-62
Ge, Fengxia; Walewski, José L; Torghabeh, Mehyar Hefazi et al. (2016) Facilitated long chain fatty acid uptake by adipocytes remains upregulated relative to BMI for more than a year after major bariatric surgical weight loss. Obesity (Silver Spring) 24:113-22
Walewski, José L; Ge, Fengxia; Lobdell 4th, Harrison et al. (2014) Spexin is a novel human peptide that reduces adipocyte uptake of long chain fatty acids and causes weight loss in rodents with diet-induced obesity. Obesity (Silver Spring) 22:1643-52
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Hu, Chunguang; Ge, Fengxia; Hyodo, Eiichi et al. (2013) Chronic ethanol consumption increases cardiomyocyte fatty acid uptake and decreases ventricular contractile function in C57BL/6J mice. J Mol Cell Cardiol 59:30-40
Clugston, Robin D; Jiang, Hongfeng; Lee, Man Xia et al. (2012) Altered hepatic retinyl ester concentration and acyl composition in response to alcohol consumption. Biochim Biophys Acta 1831:1276-86
Bradbury, Michael W; Stump, Decherd; Guarnieri, Frank et al. (2011) Molecular modeling and functional confirmation of a predicted fatty acid binding site of mitochondrial aspartate aminotransferase. J Mol Biol 412:412-22
Walewski, Jose L; Ge, Fengxia; Gagner, Michel et al. (2010) Adipocyte accumulation of long-chain fatty acids in obesity is multifactorial, resulting from increased fatty acid uptake and decreased activity of genes involved in fat utilization. Obes Surg 20:93-107
Ge, Fengxia; Lobdell 4th, Harrison; Zhou, Shengli et al. (2010) Digital analysis of hepatic sections in mice accurately quantitates triglycerides and selected properties of lipid droplets. Exp Biol Med (Maywood) 235:1282-6

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